CN112242553B - Solid-state composite electrolyte and preparation method thereof - Google Patents
Solid-state composite electrolyte and preparation method thereof Download PDFInfo
- Publication number
- CN112242553B CN112242553B CN201910650835.4A CN201910650835A CN112242553B CN 112242553 B CN112242553 B CN 112242553B CN 201910650835 A CN201910650835 A CN 201910650835A CN 112242553 B CN112242553 B CN 112242553B
- Authority
- CN
- China
- Prior art keywords
- lithium
- solid
- salt
- composite electrolyte
- electrolyte
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000003792 electrolyte Substances 0.000 title claims abstract description 149
- 239000002131 composite material Substances 0.000 title claims abstract description 96
- 238000002360 preparation method Methods 0.000 title claims abstract description 29
- 229920002749 Bacterial cellulose Polymers 0.000 claims abstract description 64
- 239000005016 bacterial cellulose Substances 0.000 claims abstract description 64
- 239000002608 ionic liquid Substances 0.000 claims abstract description 56
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 40
- 229910003002 lithium salt Inorganic materials 0.000 claims abstract description 34
- 159000000002 lithium salts Chemical class 0.000 claims abstract description 33
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 31
- 238000000498 ball milling Methods 0.000 claims description 42
- -1 imidazole imine salts Chemical class 0.000 claims description 31
- 150000003839 salts Chemical class 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 239000001301 oxygen Substances 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 10
- QSZMZKBZAYQGRS-UHFFFAOYSA-N lithium;bis(trifluoromethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F QSZMZKBZAYQGRS-UHFFFAOYSA-N 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 8
- 229910003473 lithium bis(trifluoromethanesulfonyl)imide Inorganic materials 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 239000012298 atmosphere Substances 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- JFYZBXKLRPWSGV-UHFFFAOYSA-N 1-methyl-3-propyl-2h-imidazole Chemical compound CCCN1CN(C)C=C1 JFYZBXKLRPWSGV-UHFFFAOYSA-N 0.000 claims description 3
- VDVLPSWVDYJFRW-UHFFFAOYSA-N lithium;bis(fluorosulfonyl)azanide Chemical compound [Li+].FS(=O)(=O)[N-]S(F)(=O)=O VDVLPSWVDYJFRW-UHFFFAOYSA-N 0.000 claims description 3
- 239000007774 positive electrode material Substances 0.000 claims description 3
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical group CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 claims description 2
- KAIPKTYOBMEXRR-UHFFFAOYSA-N 1-butyl-3-methyl-2h-imidazole Chemical compound CCCCN1CN(C)C=C1 KAIPKTYOBMEXRR-UHFFFAOYSA-N 0.000 claims description 2
- IBZJNLWLRUHZIX-UHFFFAOYSA-N 1-ethyl-3-methyl-2h-imidazole Chemical compound CCN1CN(C)C=C1 IBZJNLWLRUHZIX-UHFFFAOYSA-N 0.000 claims description 2
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 2
- 125000002152 1H-pyrrolizinyl group Chemical class C1(C=CN2C=CC=C12)* 0.000 claims description 2
- 229910012851 LiCoO 2 Inorganic materials 0.000 claims description 2
- 229910010707 LiFePO 4 Inorganic materials 0.000 claims description 2
- 229910015872 LiNi0.8Co0.1Mn0.1O2 Inorganic materials 0.000 claims description 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 7
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 abstract description 6
- 230000003993 interaction Effects 0.000 abstract description 6
- 150000002500 ions Chemical class 0.000 abstract description 6
- 229910001416 lithium ion Inorganic materials 0.000 abstract description 6
- 238000013508 migration Methods 0.000 abstract description 5
- 230000005012 migration Effects 0.000 abstract description 5
- 238000010494 dissociation reaction Methods 0.000 abstract description 3
- 230000005593 dissociations Effects 0.000 abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 3
- 239000007791 liquid phase Substances 0.000 abstract description 3
- 239000007790 solid phase Substances 0.000 abstract description 3
- 230000001737 promoting effect Effects 0.000 abstract description 2
- 150000001450 anions Chemical class 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 13
- 239000012528 membrane Substances 0.000 description 13
- 239000012300 argon atmosphere Substances 0.000 description 12
- 239000007788 liquid Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 7
- 229920000831 ionic polymer Polymers 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000007772 electrode material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000011056 performance test Methods 0.000 description 4
- 239000007784 solid electrolyte Substances 0.000 description 4
- 238000011161 development Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- HLNRRPIYRBBHSQ-UHFFFAOYSA-N 1-propylpyrrolidine Chemical compound CCCN1CCCC1 HLNRRPIYRBBHSQ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- ZXAKFAMWSBPGHR-UHFFFAOYSA-N CCCN1CCCC1.O=S(C(F)(F)F)(NS(C(F)(F)F)(=O)=O)=O Chemical compound CCCN1CCCC1.O=S(C(F)(F)F)(NS(C(F)(F)F)(=O)=O)=O ZXAKFAMWSBPGHR-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000002001 electrolyte material Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- MCVFFRWZNYZUIJ-UHFFFAOYSA-M lithium;trifluoromethanesulfonate Chemical compound [Li+].[O-]S(=O)(=O)C(F)(F)F MCVFFRWZNYZUIJ-UHFFFAOYSA-M 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000005463 sulfonylimide group Chemical group 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- ZJPPTKRSFKBZMD-UHFFFAOYSA-N [Li].FS(=N)F Chemical compound [Li].FS(=N)F ZJPPTKRSFKBZMD-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000011244 liquid electrolyte Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000005486 organic electrolyte Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000012716 precipitator Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0017—Non-aqueous electrolytes
- H01M2300/0065—Solid electrolytes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Conductive Materials (AREA)
- Secondary Cells (AREA)
Abstract
The invention belongs to the technical field of lithium secondary batteries, in particular to a lithium secondary batteryA solid-state composite electrolyte and a preparation method thereof. The solid-state composite electrolyte comprises bacterial cellulose, lithium salt and ionic liquid; the composite electrolyte can be used in a battery; the solid-state composite electrolyte has a large number of hydroxyl groups in bacterial cellulose macromolecular chains, and can be matched with anion TFSI ‑ N of (a) ‑ The interaction generates hydrogen bonds, thereby further promoting the dissociation of lithium salt, facilitating the migration of lithium ions and improving the ion conductivity of the electrolyte; the solid-state composite electrolyte provided by the invention has the excellent performances of liquid-phase electrolyte and solid-phase electrolyte, and the ionic liquid and the bacterial cellulose can form the solid-state composite electrolyte with stable structure through hydrogen bond interaction.
Description
Technical Field
The invention belongs to the technical field of lithium secondary batteries, and particularly relates to a solid-state composite electrolyte and a preparation method thereof.
Background
With the continuous development of new energy storage devices, lithium secondary batteries are becoming an indispensable part of the current development of new energy as a main medium for the storage and conversion of new energy. The electrolyte is an important component of the battery, plays an important role in ion transmission in the battery, and has a great influence on the service performance of the battery. However, most of the current commercial lithium secondary batteries use liquid organic electrolyte, and have the problems of flammability, explosiveness, environmental pollution, limited use conditions and the like. The solid electrolyte material comprises two parts: one part is active liquid component and mainly responsible for ion conduction; the other part is an inert solid framework, which is mainly responsible for providing enough specific surface area and mechanical support for the adhesion of liquid components. The electrolyte solves the defects of the liquid electrolyte to a certain extent, and becomes a hot spot of current research.
However, the solid electrolyte materials are widely selected and have different synthesis methods, so how to screen and optimize the most suitable materials is a problem to be solved by the quasi-solid composite electrolyte applied to the lithium secondary battery at present.
There are many solid matrix materials reported in the prior art to be used in solid-state composite electrolytes, such as a composite electrolyte comprising bacterial cellulose (bacterial cellulose, BC) as a substrate for mixing Li 7 La 3 Zr 2 O 12 And poly (ethylene oxide) (PEO) composite electrolytes, which have good mechanical properties, but the preparation method of the electrolyte is cumbersome, the ionic conductivity is low, and it is difficult to use in a high temperature environment (adv. Energy mate.2018, 1703474). As in chinese patent document CN108232085a, a bacterial cellulose membrane and a preparation method thereof are disclosed, wherein a layer of polyion liquid is coated on the surface of the bacterial cellulose membrane, the preparation method comprises the steps of firstly placing the bacterial cellulose membrane in a polyion liquid aqueous solution, impregnating to enable the bacterial cellulose membrane to adsorb polyion liquid, then placing the membrane in a precipitator, obtaining a polyion liquid coated bacterial cellulose membrane after impregnation, finally placing the bacterial cellulose membrane in a lithium salt solution, impregnating to obtain a polyion liquid coated bacterial cellulose membrane after anion exchange, and obtaining a polyion liquid coated bacterial cellulose membrane after hot pressing and drying; the bacterial cellulose membrane prepared by the patent has the advantage of good thermal stability when used as a membrane in a battery, but the membrane taking the bacterial cellulose membrane as a matrix needs to be added with a toxic precipitant such as acetone and the like in the preparation process, and has the effect of protecting human bodiesHarmful, and the preparation process requires a long time and is cumbersome.
Disclosure of Invention
Therefore, the technical problem to be solved by the invention is to overcome the defects that the solid electrolyte in the prior art is poor in physical and chemical properties, difficult to simultaneously have thermal stability and high ionic conductivity, complex in preparation method, long in time consumption, easy to introduce impurities and the like, so that the solid composite electrolyte and the preparation method thereof are provided.
For this purpose, the invention provides the following technical scheme.
The invention provides a solid-state composite electrolyte, which comprises bacterial cellulose, lithium salt and ionic liquid;
the ionic liquid is monomer imidazole imine salts and/or monomer pyrrole imine salts.
The mass ratio of the bacterial cellulose to the ionic liquid electrolyte is 1: (1.5-2.5);
the ionic liquid electrolyte comprises ionic liquid and lithium salt, wherein the dosage of the lithium salt is 0.2-1.2mol based on 1L of the ionic liquid.
The lithium salt is at least one of lithium bisoxalato borate, lithium difluorooxalato borate, lithium trifluoromethane sulfonate, lithium bistrifluoromethane sulfonyl imide, lithium bisfluoro sulfonyl imide, lithium perfluoro ethane sulfonyl imide and lithium perfluoro methane sulfonyl methyl.
The imidazole imine salt is at least one of 1-ethyl-3-methylimidazole bis (trifluoromethyl) sulfonyl imide salt, 1-propyl-3-methylimidazole bis (trifluoromethyl) sulfonyl imide salt, 1-butyl-3-methylimidazole bis (trifluoromethyl) sulfonyl imide salt, 1-ethyl-3-methylimidazole bis (fluoro) sulfonyl imide salt, 1-propyl-3-methylimidazole bis (fluoro) sulfonyl imide salt and 1-butyl-3-methylimidazole bis (fluoro) sulfonyl imide salt;
the pyrrolizine salt is at least one of N-methyl, propyl pyrrole bis (trifluoromethyl) sulfonyl imide salt, N-methyl, butyl pyrrole bis (trifluoromethyl) sulfonyl imide salt, N-methyl, propyl pyrrole bis (fluoro) sulfonyl imide salt and N-methyl and butyl pyrrole bis (fluoro) sulfonyl imide salt.
The invention provides a preparation method of solid-state composite electrolyte, which comprises the steps of uniformly mixing lithium salt and ionic liquid to form ionic liquid electrolyte, adding 50-300 meshes of bacterial cellulose, and ball milling to obtain the solid-state composite electrolyte.
Further, the rotation speed of the ball mill is 300-400 r.min -1 Ball milling time is 3-6h.
The mixing of the lithium salt and the ionic liquid is carried out under inert or nitrogen atmosphere;
the moisture content of the atmosphere is less than 0.1ppm;
the oxygen content of the atmosphere is less than 0.1ppm.
The invention provides an application of the solid-state composite electrolyte or the solid-state composite electrolyte prepared by the method in a lithium secondary battery.
The positive electrode material of the lithium secondary battery may be, but is not limited to, liFePO 4 、LiCoO 2 、LiNi 0.8 Co 0.1 Mn 0.1 O 2 And the like.
The technical scheme of the invention has the following advantages:
1. the solid-state composite electrolyte provided by the invention comprises bacterial cellulose, lithium salt and ionic liquid; the composite electrolyte does not contain impurities, belongs to solid electrolyte, and can be used in batteries; the solid-state composite electrolyte has a large number of hydroxyl groups in bacterial cellulose macromolecular chains, and can be matched with TFSI in ionic liquid - N in (imine bond) - The interaction generates hydrogen bonds, thereby further promoting the dissociation of lithium salt, facilitating the migration of lithium ions and improving the ion conductivity of the electrolyte; as the bacterial cellulose, lithium salt and ionic liquid have good high temperature resistance, the thermal decomposition temperature of the solid-state composite electrolyte can reach 300 ℃, and the solid-state composite electrolyte has good high temperature performance;
the solid-state composite electrolyte has the excellent performances of liquid-phase electrolyte and solid-phase electrolyte, and the ionic liquid and the bacterial cellulose can form the solid-state composite electrolyte with stable structure through hydrogen bond interaction, and the ionic liquid electrolyte is present, so that the solid-state composite electrolyte provided by the invention can infiltrate the electrode material better, the interface compatibility of the solid-state electrolyte and the electrode material is improved, and the interface impedance is reduced;
the bacterial cellulose in the solid-state composite electrolyte has the characteristics of large specific surface area, high porosity, high mechanical strength, good shape maintenance capability and the like, the large specific surface area can provide a large number of attachment sites for the ionic liquid electrolyte, and a large number of unordered porous structures in the electrolyte can provide channels for lithium ion migration;
in addition, the solid-state composite electrolyte has good mechanical property and strong flexibility, is easy to process and form, and can be suitable for being matched with various positive electrode materials and applied to lithium secondary batteries.
2. According to the solid-state composite electrolyte provided by the invention, the bacterial cellulose, the ionic liquid and the lithium salt are regulated in use amount, so that the solid-state composite electrolyte material with a proper proportion is obtained, and the solid-state composite electrolyte material has good chemical and electrochemical properties.
At least one of lithium bisoxalato borate, lithium difluorooxalato borate, lithium trifluoromethane sulfonate, lithium bistrifluoromethane sulfonyl imide, lithium bisfluoro sulfonyl imide, lithium perfluoroethane sulfonyl imide and lithium perfluoromethane sulfonyl methyl as a lithium salt, wherein N in the imine lithium salt - The hydroxyl groups in the bacterial cellulose are easy to form hydrogen bonds, so that the migration of lithium ions is promoted, and the ion conductivity of the electrolyte is improved.
3. The preparation method of the solid-state composite electrolyte provided by the invention comprises the steps of uniformly mixing lithium salt and ionic liquid, adding bacterial cellulose, and performing ball milling to obtain the solid-state composite electrolyte, wherein the preparation method is simple, easy to operate, short in time consumption and low in cost, no impurities are required to be introduced in the preparation process, and conventional equipment is used, so that the solid-state composite electrolyte is suitable for large-scale batch production; in the ball milling process, the ionic liquid electrolyte can enter into a disordered porous skeleton of the bacterial cellulose and generate hydrogen bond interaction with the bacterial cellulose, so that the ion migration rate can be further improved, and the material structure is more stable.
4. The solid-state composite electrolyte can be applied as electrolyte in a lithium secondary battery, and the composite electrolyte does not need to be added with a diaphragm and electrolyte when in application, and is convenient and simple in practical application and higher in safety.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings that are needed in the description of the embodiments or the prior art will be briefly described, and it is obvious that the drawings in the description below are some embodiments of the present invention, and other drawings can be obtained according to the drawings without inventive effort for a person skilled in the art.
FIG. 1 is a scanning electron microscope image of bacterial cellulose of example 8 of the present invention;
FIG. 2 is a scanning electron microscope image of the solid-state composite electrolyte of example 8 in the present invention;
FIG. 3 is a thermogravimetric analysis graph of bacterial cellulose, ionic liquid electrolyte and novel solid state composite electrolyte based on bacterial cellulose according to example 8 of the present invention;
fig. 4 is a charge and discharge graph of CR2025 type lithium secondary batteries having a composite electrolyte composition prepared in example 8 according to the present invention at various temperatures.
Detailed Description
The following examples are provided for a better understanding of the present invention and are not limited to the preferred embodiments described herein, but are not intended to limit the scope of the invention, any product which is the same or similar to the present invention, whether in light of the present teachings or in combination with other prior art features, falls within the scope of the present invention.
The specific experimental procedures or conditions are not noted in the examples and may be followed by the operations or conditions of conventional experimental procedures described in the literature in this field. The reagents or apparatus used were conventional reagent products commercially available without the manufacturer's knowledge.
Example 1
This example provides a solid-state composite electrolyte comprising 0.2372g of lithium bis-fluorosulfonyl imide, 1.7628g N-methyl, propylpyrrolidine bis-trifluoromethanesulfonyl imide salt (density 1.39g cm) -3 ) And 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.2372g of lithium bis (fluorosulfonyl) imide is weighed in 1.7628g N-methyl, propyl pyrrolidine bis (trifluoromethanesulfonyl) imide salt, and the mixture is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 2
The embodiment provides a solid-state composite electrolyte comprising 0.3181g of lithium bistrifluoromethane sulfonyl imide and 1.6819g of 1-ethyl-3-methylimidazole bistrifluoromethane sulfonyl imide salt (density 1.518 g.cm) -3 ) And 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
0.3181g of lithium bistrifluoromethane sulfonyl imide is weighed in 1.6819g of 1-ethyl-3-methylimidazole bistrifluoromethane sulfonyl imide salt in a glove box with the argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, and the mixture is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 3
The present example provides a solid-state composite electrolyte comprising 0.2127g of lithium bistrifluoromethane sulfonimide, 1.2873g N-methyl, propylpyrrolidine bistrifluoromethane sulfonimide salt and 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.2127g of lithium bistrifluoromethane sulfonyl imide is weighed in 1.2873g N-methyl, and the lithium bistrifluoromethane sulfonyl imide salt is continuously stirred until the lithium salt is completely dissolved, thus obtaining 0.8mol.L -1 An ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 4
The present example provides a solid-state composite electrolyte comprising 0.2568g of lithium bistrifluoromethane sulfonimide, 1.2432g N-methyl, propylpyrrolidine bistrifluoromethane sulfonimide salt and 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.2568g of lithium bistrifluoromethane sulfonyl imide is weighed in 1.2432g N-methyl, and the lithium bistrifluoromethane sulfonyl imide salt is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 5
This example provides a composite electrolyte comprising 0.2979g of lithium bis (trifluoromethanesulfonyl) imide, 1.2021g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 1g of bacterial cellulose;
the preparation method of the composite electrolyte comprises the steps of,
in an argon atmosphere and waterIn a glove box with the content of the lithium bistrifluoromethane sulfonyl imide and the oxygen content of less than 0.1ppm, 0.2979g of lithium bistrifluoromethane sulfonyl imide is weighed in 1.2021g N-methyl, and the lithium bistrifluoromethane sulfonyl imide salt is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1.2 mol.L -1 An ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 6
This example provides a solid-state composite electrolyte comprising 0.1712g lithium bis (trifluoromethanesulfonyl) imide, 0.8288g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 0.625g bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1712g of lithium bistrifluoromethane sulfonyl imide is weighed in 0.8288-g N-methyl, propyl pyrrolidine bistrifluoromethane sulfonyl imide salt and is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
0.625g bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 7
This example provides a solid-state composite electrolyte comprising 0.1712g lithium bis (trifluoromethanesulfonyl) imide, 0.8288g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 0.5714g bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1712g of lithium bistrifluoromethane sulfonyl imide is weighed in 0.8288-g N-methyl, propyl pyrrolidine bistrifluoromethane sulfonyl imide salt and is continuously stirred until the lithium salt is completely dissolvedDissolving to obtain 1 mol.L -1 An ionic liquid electrolyte;
weighing 0.5714g of bacterial cellulose powder with 200 meshes, placing the bacterial cellulose powder into a ball milling tank, adding the ionic liquid electrolyte, sealing the ball milling tank, and performing ball milling for 4 hours at the rotating speed of 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 8
This example provides a solid-state composite electrolyte comprising 0.1712g lithium bis (trifluoromethanesulfonyl) imide, 0.8288g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 0.5g bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1712g of lithium bistrifluoromethane sulfonyl imide is weighed in 0.8288-g N-methyl, propyl pyrrolidine bistrifluoromethane sulfonyl imide salt and is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
0.5g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 9
This example provides a solid-state composite electrolyte comprising 0.1712g lithium bis (trifluoromethanesulfonyl) imide, 0.8288g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 0.4444g bacterial cellulose;
the preparation method of the composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1712g of lithium bistrifluoromethane sulfonyl imide is weighed in 0.8288-g N-methyl, propyl pyrrolidine bistrifluoromethane sulfonyl imide salt and is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
0.4444g of 180-mesh bacterial cellulose powder is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, and the balls are formedBall milling is carried out for 4 hours after the grinding tank is sealed, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 10
This example provides a solid-state composite electrolyte comprising 0.1712g lithium bis (trifluoromethanesulfonyl) imide, 0.8288g N-methyl, propylpyrrolidine bis (trifluoromethanesulfonyl) imide salt and 0.4g bacterial cellulose;
the preparation method of the composite electrolyte comprises the steps of,
in a glove box with an argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1712g of lithium bistrifluoromethane sulfonyl imide is weighed in 0.8288-g N-methyl, propyl pyrrolidine bistrifluoromethane sulfonyl imide salt and is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 An ionic liquid electrolyte;
0.4g of bacterial cellulose powder with 230 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 11
The embodiment provides a solid-state composite electrolyte, which comprises 0.1117g of lithium difluorosulfimide, 0.1526g of lithium difluorooxalato borate, 0.8297g N-methyl, propylpyrrolidine bistrifluoromethylsulfonimide salt and 0.9060g of 1-ethyl-3-methylimidazole bistrifluoromethylsulfonimide salt (density of 1.518 g.cm) -3 ) 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1117g of lithium bis (fluorosulfonyl) imide and 0.1526g of lithium difluoro (oxalato) borate are weighed in 0.8297g N-methyl, propyl pyrrolidine bis (trifluoromethylsulfonyl) imide salt and 0.9060g of 1-ethyl-3-methylimidazole bis (trifluoromethylsulfonyl) imide salt, and stirring is continued until the two lithium salts are completely dissolved, thus obtaining 1 mol.L -1 Mixing an ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, and ball milling is carried outBall milling is carried out for 4 hours after sealing the tank, and the rotating speed is 300 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Example 12
This example provides a solid-state composite electrolyte comprising 0.1031g of perfluoromethanesulfonyl methyl lithium and 0.1533g of lithium difluorooxalato borate, 0.8592g of 1-butyl-3-methylimidazole bistrifluoromethanesulfonyl imide salt (density 1.433g cm) -3 ) And 0.8844g of 1-propyl-3-methylimidazole bis-fluoromethanesulfonimide salt (density 1.475g cm) -3 ) 1g of bacterial cellulose;
the preparation method of the solid-state composite electrolyte comprises the steps of,
in a glove box with argon atmosphere and the moisture content and the oxygen content of less than 0.1ppm, 0.1031g of perfluoromethane sulfonyl methyl lithium and 0.1533g of lithium difluorooxalato borate are weighed in 0.8592g of 1-butyl-3-methylimidazole bis (trifluoromethane sulfonyl) imide salt and 0.8844g of 1-propyl-3-methylimidazole bis (fluoromethanesulfonyl) imide salt, and the mixture is continuously stirred until the lithium salt is completely dissolved, thus obtaining 1 mol.L -1 Mixing an ionic liquid electrolyte;
1g of bacterial cellulose powder with 200 meshes is weighed and placed in a ball milling tank, then the ionic liquid electrolyte is added, the ball milling tank is sealed and ball milled for 4 hours, and the rotating speed is 400 r.min -1 And ball milling to obtain the solid-state composite electrolyte.
Test examples
The test examples provided the application, performance test and test results of the solid-state composite electrolytes prepared in examples 1 to 12, the test methods are as follows, and the test results are shown in Table 1;
the solid-state composite electrolytes of examples 1 to 12 were used as electrolytes in lithium secondary batteries, and the specific steps of assembling the lithium secondary batteries include the steps of incorporating active electrode materials LiFePO 4 Mixing acetylene black and polyvinylidene fluoride according to the mass ratio of 8:1:1, then dropwise adding 5 drops of N-methyl pyrrolidone, and grinding into uniform slurry; uniformly coating the slurry on a current collector aluminum foil, placing the current collector aluminum foil in a vacuum drying oven at 80 ℃ for drying for 24 hours, and then rolling and punching to obtain an electrode plate with the thickness of 100 mu m and the diameter of 11 mm; in a glove box filled with argon, the electrode plate is put into practiceThe solid-state composite electrolytes and metallic lithium sheets prepared in examples 1 to 12 were sequentially placed in a button cell case of 2025, and then compacted and fastened by a tablet press to obtain a lithium secondary battery.
The morphology of the solidified composite electrolyte was tested using a scanning electron microscope model HITACHI S-4800 (japan);
the thermal stability of the solid-stating composite electrolyte was tested using a thermogravimetric analyzer model Netzsch STA 499F3 (germany);
the lithium secondary battery was subjected to a charge and discharge performance test using a LAND battery test system of model CT2001A (china), and the charge and discharge performance tests were performed at different temperatures at a current density of 0.1C, and the test results are shown in table 1;
TABLE 1 results of charge-discharge Performance test of lithium secondary batteries prepared from the composite electrolytes prepared in examples 1 to 12 as electrolytes
As shown in table 1, the solid-state composite electrolyte prepared by the invention shows good cycle performance and higher specific capacity after being matched with a lithium ion battery, and has higher coulombic efficiency of first-week charge and discharge, thus proving that the electrolyte has better electrochemical performance and development potential applied to the solid-state battery;
as can be seen from fig. 4, the solid-state composite electrolyte prepared in example 8 has standard long and flat charge-discharge platform under different temperatures, and the polarization voltage is smaller and smaller along with the temperature rise, which indicates that the solid-state composite electrolyte provided in the invention has better interface compatibility with the electrode material, is suitable for use at higher temperature, has good cycle stability, and can be applied to lithium secondary batteries for a long time.
As can be seen from fig. 1 and fig. 2, SEM test results show that the Bacterial Cellulose (BC) in the composite electrolyte in example 8 has a plurality of cross-linked network structures, and has a large specific surface area, which is beneficial to the uniform adhesion of the ionic liquid electrolyte in the interior and on the surface thereof, and is beneficial to the transmission of lithium ions; SEM images of the composite electrolyte show that the liquid phase and the solid phase materials are tightly combined, and the structure of the electrolyte is extremely stable due to the interaction of hydrogen bonds, so that the dissociation of lithium salt is further promoted.
FIG. 3 shows that the bacterial cellulose and the ionic liquid electrolyte in example 8 have good thermal stability, and the obtained solid-state composite electrolyte has only a small mass loss at the temperature lower than 300 ℃ and the thermal decomposition temperature can reach 300 ℃; BC-ILE-2 is expressed as a mass ratio of ILE to BC of 2:1.
Therefore, the solid-state composite electrolyte prepared by the invention has better electrochemical performance, high-temperature stability and high ionic conductivity, and the preparation method is simple and easy to operate.
It is apparent that the above examples are given by way of illustration only and are not limiting of the embodiments. Other variations or modifications of the above teachings will be apparent to those of ordinary skill in the art. It is not necessary here nor is it exhaustive of all embodiments. And obvious variations or modifications thereof are contemplated as falling within the scope of the present invention.
Claims (8)
1. A solid-state composite electrolyte, comprising bacterial cellulose and an ionic liquid electrolyte;
the ionic liquid electrolyte comprises ionic liquid and lithium salt, wherein the dosage of the lithium salt is 0.2-1.2mol based on 1L of the ionic liquid;
the ionic liquid is monomer imidazole imine salts and/or monomer pyrrole imine salts;
the mass ratio of the bacterial cellulose to the ionic liquid electrolyte is 1: (1.5-2.5).
2. The solid-state composite electrolyte according to claim 1, wherein the lithium salt is at least one of lithium bis (oxalato) borate, lithium difluoro (oxalato) borate, lithium trifluoro (methanesulfonyl) sulfonate, lithium bis (trifluoromethanesulfonyl) imide, lithium bis (fluorosulfonyl) imide, lithium perfluoroethanesulfonyl imide, and lithium perfluoromethanesulfonylmethyl.
3. The solid-state composite electrolyte according to claim 1 or 2, wherein the imidazole imine salt is at least one of 1-ethyl-3-methylimidazole bis-trifluoromethanesulfonyl imide salt, 1-propyl-3-methylimidazole bis-trifluoromethanesulfonyl imide salt, 1-butyl-3-methylimidazole bis-trifluoromethanesulfonyl imide salt, 1-ethyl-3-methylimidazole bis-fluoromethanesulfonyl imide salt, 1-propyl-3-methylimidazole bis-fluoromethanesulfonyl imide salt, and 1-butyl-3-methylimidazole bis-fluoromethanesulfonyl imide salt;
the pyrrolizine salt is at least one of N-methyl, propyl pyrrole bis (trifluoromethyl) sulfonyl imide salt, N-methyl, butyl pyrrole bis (trifluoromethyl) sulfonyl imide salt, N-methyl, propyl pyrrole bis (fluoro) sulfonyl imide salt and N-methyl and butyl pyrrole bis (fluoro) sulfonyl imide salt.
4. A method for preparing the solid-state composite electrolyte according to any one of claims 1 to 3, which is characterized by comprising the steps of uniformly mixing lithium salt and ionic liquid to form the ionic liquid electrolyte, adding bacterial cellulose with 50 to 300 meshes, and performing ball milling to obtain the solid-state composite electrolyte.
5. The method according to claim 4, wherein the rotational speed of the ball mill is 300-400r/min and the ball milling time is 3-6h.
6. The preparation method according to claim 4 or 5, wherein the mixing of the lithium salt with the ionic liquid is performed under an inert or nitrogen atmosphere;
the moisture content of the atmosphere is less than 0.1ppm;
the oxygen content of the atmosphere is less than 0.1ppm.
7. Use of the solid-state composite electrolyte according to any one of claims 1 to 3 or the solid-state composite electrolyte prepared by the method according to any one of claims 4 to 6 in a lithium secondary battery.
8. The use according to claim 7, wherein the positive electrode material of the lithium secondary battery is LiFePO 4 、LiCoO 2 Or LiNi 0.8 Co 0.1 Mn 0.1 O 2 。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910650835.4A CN112242553B (en) | 2019-07-18 | 2019-07-18 | Solid-state composite electrolyte and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910650835.4A CN112242553B (en) | 2019-07-18 | 2019-07-18 | Solid-state composite electrolyte and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN112242553A CN112242553A (en) | 2021-01-19 |
| CN112242553B true CN112242553B (en) | 2024-03-19 |
Family
ID=74168338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201910650835.4A Active CN112242553B (en) | 2019-07-18 | 2019-07-18 | Solid-state composite electrolyte and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112242553B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7155186B2 (en) * | 2020-03-23 | 2022-10-18 | 株式会社東芝 | Composite electrolyte, secondary battery, battery pack and vehicle |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101585931A (en) * | 2008-05-23 | 2009-11-25 | 中国科学院化学研究所 | Compound polymer electrolyte material and preparation method and application thereof |
| CN108232085A (en) * | 2017-12-25 | 2018-06-29 | 佛山市东航光电科技股份有限公司 | Poly ion liquid coated bacteria cellulose membrane and preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9985313B2 (en) * | 2014-01-02 | 2018-05-29 | Wildcat Discovery Technologies, Inc. | Solid state electrolyte and electrode compositions |
-
2019
- 2019-07-18 CN CN201910650835.4A patent/CN112242553B/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101585931A (en) * | 2008-05-23 | 2009-11-25 | 中国科学院化学研究所 | Compound polymer electrolyte material and preparation method and application thereof |
| CN108232085A (en) * | 2017-12-25 | 2018-06-29 | 佛山市东航光电科技股份有限公司 | Poly ion liquid coated bacteria cellulose membrane and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN112242553A (en) | 2021-01-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Zhang et al. | Water-soluble polyacrylic acid as a binder for sulfur cathode in lithium-sulfur battery | |
| CN102709597B (en) | Composite all solid-state polymer electrolyte lithium ion battery and preparation method of composite all solid-state polymer electrolyte lithium ion battery | |
| CN107681091B (en) | Lithium-sulfur battery functional composite diaphragm and preparation method thereof | |
| CN106058312B (en) | A kind of solid state ionic liquid electrolyte, preparation method and application | |
| CN102916195B (en) | Graphene-coated copper oxide composite cathode material and method for manufacturing same | |
| CN100478390C (en) | Compound polymer electrolytic material and preparation method thereof | |
| CN104934579B (en) | A kind of porous graphite doping and the preparation method of carbon coating graphite cathode material | |
| CN104157909B (en) | A kind of preparation method of lithium-sulfur cell membrane electrode | |
| CN107342412B (en) | Preparation method of nano microsphere phosphotungstate/sulfur positive electrode material | |
| CN111725559B (en) | Solid electrolyte, method for preparing the same, and lithium secondary solid battery | |
| CN108933047A (en) | A kind of prelithiation gel electrolyte and preparation method thereof for lithium-ion capacitor | |
| CN114335701A (en) | Composite solid electrolyte membrane and preparation method thereof | |
| CN105185978A (en) | Manganese-containing oxygen compound used as negative active substance, and preparation method and use thereof | |
| CN108878777B (en) | Single-ion-conducting polymer lithium-sulfur battery | |
| CN111799502B (en) | Garnet type solid composite electrolyte, preparation method and application | |
| CN108550818A (en) | A kind of lithium sulfur battery anode material and its application | |
| CN112242553B (en) | Solid-state composite electrolyte and preparation method thereof | |
| CN114447321A (en) | Positive electrode material, positive plate comprising same and battery | |
| CN103490071B (en) | Lithium-Polyaniline Secondary Battery and preparation method thereof | |
| CN108923033B (en) | Preparation method of porous carbon cathode material of lithium-sulfur battery based on phase transfer method | |
| CN114725309B (en) | Preparation method of high-performance composite conductive paste for lithium battery | |
| CN116443941A (en) | Preparation and application of in-situ carbon-coated sodium ferric sulfate positive electrode material | |
| CN109873157A (en) | Co for lithium ion battery2(BDC)2Ted negative electrode material | |
| CN110635174A (en) | Preparation method of three-dimensional lithium ion battery | |
| CN114512710A (en) | Coated sulfide solid electrolyte material and preparation method and application thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |